Objective:Posterior capsular opacification(PCO) is the main complication of modern cataract surgery and cause of poor vision post-operation.Residual lens epithelial cells (LECs) undergo epithelial mesenchymal transition(EMT) in the progress of PCO. Previous work has revealed that transforming growth factor beta(TGF-β)play an important role in PCO.Though it is extensively studied,the mechanism of TGF-βon lens is complex and not completely understood yet.Connective tissue growth factor (CTGF) is a matricellular protein that has been found to participate in EMT.So it is critical to understand the mechanism of CTGF,a potent growth factor in ocular media, in process of EMT in LECs.On the basis of previous studies,we established a research model for PCO in vitro.We also took the siRNA technique to selectively silence the expression of CTGF in LECs to investigate the role of CTGF in TGF-β2 induced EMT in human lens epithelial cells.Methods:HLE B-3 cells were treated with different concentrations of TGF-β2 to investigate effect of TGF-β2 on expression of CTGF,connexin43 and a-SMA with western blot and RT-PCR.siRNA technique was operated to selectively silence the expression of CTGF gene.Then we analyzed the effect of siRNA interfere on TGF-β2 induced EMT and adhesion of LECs with western blot and immunofluorescence.Results:HLE B-3 cells underwent morphological alteration and EMT under TGF-β2 stimulation concomitant with dramatic up-regulation of CTGF mRNA and protein levels.The expression of Connexin43 was decreased after treatment of TGF-β2,while the expression of a-SMA was increased.CTGF silencing by CTGF siRNA approaches showed that TGF-β2-induced EMT and adhesion were CTGF dependent.Conclusion:CTGF is an essential downstream mediator of TGF-β2-induced EMT in lens epithelial ceils.Selectively silence the expression of CTGF could be a potent therapeutic target of PCO. |